List of variants in gene FKBP10 reported as uncertain significance by Eurofins NTD LLC (GA)

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 16

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_021939.4(FKBP10):c.1667G>A (p.Arg556His)	rs138281924	0.00120
NM_021939.4(FKBP10):c.174A>G (p.Glu58=)	rs150052125	0.00083
NM_021939.4(FKBP10):c.473T>C (p.Val158Ala)	rs781874365	0.00009
NM_021939.4(FKBP10):c.429T>G (p.Asp143Glu)	rs141427325	0.00007
NM_021939.4(FKBP10):c.1269G>A (p.Gly423=)	rs371540139	0.00006
NM_021939.4(FKBP10):c.315C>T (p.Gly105=)	rs373064272	0.00004
NM_021939.4(FKBP10):c.1063+6G>A	rs1555616698	0.00001
NM_021939.4(FKBP10):c.1160G>A (p.Arg387Gln)	rs782107514	0.00001
NM_021939.4(FKBP10):c.1208G>A (p.Arg403Gln)	rs886044826	0.00001
NM_021939.4(FKBP10):c.1399+8G>T	rs782073490	0.00001
NM_021939.4(FKBP10):c.422A>G (p.Tyr141Cys)	rs782600573	0.00001
NM_021939.4(FKBP10):c.1029C>T (p.Ile343=)	rs782632205
NM_021939.4(FKBP10):c.1390G>A (p.Glu464Lys)	rs886044888
NM_021939.4(FKBP10):c.1550T>A (p.Val517Asp)	rs797044794
NM_021939.4(FKBP10):c.21C>T (p.Pro7=)	rs781985978
NM_021939.4(FKBP10):c.246-5C>G	rs140027863

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.